Related Experiment Video

Updated: Jun 18, 2025

A Simple and Efficient Protocol for the Catalytic Insertion Polymerization of Functional Norbornenes
09:08

A Simple and Efficient Protocol for the Catalytic Insertion Polymerization of Functional Norbornenes

Published on: February 27, 2017

10.3K

Correction to "Modular Synthetic Platform for Interior-Functionalized Dendritic Macromolecules Enabled by the

Shinyoung Choi, Ki-Young Yoon, Guangbin Dong

    Journal of the American Chemical Society
    |July 31, 2024
    PubMed
    Summary

    No abstract available in PubMed .

    More Related Videos

    Author Spotlight: Functionalizing Metal-Organic Frameworks: Advancements, Challenges, and the Power of Post-Synthetic Ligand Exchange04:51

    Author Spotlight: Functionalizing Metal-Organic Frameworks: Advancements, Challenges, and the Power of Post-Synthetic Ligand Exchange

    Published on: June 23, 2023

    2.8K
    High-throughput Synthesis of Carbohydrates and Functionalization of Polyanhydride Nanoparticles14:37

    High-throughput Synthesis of Carbohydrates and Functionalization of Polyanhydride Nanoparticles

    Published on: July 6, 2012

    11.4K

    Related Concept Videos

    [4+2] Cycloaddition of Conjugated Dienes: Diels–Alder Reaction01:16

    [4+2] Cycloaddition of Conjugated Dienes: Diels–Alder Reaction

    The Diels–Alder reaction is an example of a thermal pericyclic reaction between a conjugated diene and an alkene or alkyne, commonly referred to as a dienophile. The reaction involves a concerted movement of six π electrons, four from the diene and two from the dienophile, forming an unsaturated six-membered ring. As a result, these reactions are classified as [4+2] cycloadditions.
    10.1K